Publications by authors named "Tan Haiying"

Giving Timely warnings for fire is very crucial for fire prevention and the protection of people's lives and property. However, most current fire warning sensors give warnings above 200 °C, which are not conducive to efficient and accurate warnings. Therefore, it is important to develop high-temperature sensors that can give timely, portable warnings at low temperatures (100 to 200 °C).

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Wound dressings can generally complete hemostasis and provide temporary protection after skin damage. Herein, a MXene-based hydrogel was prepared from MXene, gelatin, poly(ethylene glycol)diacrylate (PEGDA) and ,'-methylenebis(acrylamide) (HEAA) to prepare wound-dressing hydrogels for skin repair. HEAA and PEGDA crosslink polymerization formed the first layer of the network.

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Structural coloration as the most possible way to realize the ecofriendly dying process for textiles or fabrics has attracted significant attention in the past decades. However, photonic crystals (PCs) are a typical example of materials with structural color usually located on the surface of the fabrics or textiles, which make them not stable when rubbed, bent, or washed due to the weak interaction between the PC coatings and fabrics. Here, double networks were constructed between the PC coatings and the fabrics for the first time via a hydrogen bond by introducing tannic acid (TA) and dynamic cross-linking with 2-formylphenylboronic acid to increase the wash resistance of the structural colored fabrics.

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Structural colors can be used in fabric coloring due to their bright color and non-fading properties. However, it is still a challenge to construct structural color on high crystallinity, smooth surfaced and yellow colored aramid fabrics. Herein, for the first time, photonic crystals (PCs) with structural color were constructed on aramid fabrics by introducing dopamine to modify aramid fabrics and synthesizing monodisperse high refractive index zinc sulfide nanoparticles (ZnS).

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Modification of nanorods (NRs) with functional polymer ligands is of great significance to enhance their surface chemistry and prompt their applications in many fields (e.g., photothermal therapy, bioimaging, and catalysis).

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Photonic elastomers that can change colors like a chameleon have shown great promise in various applications. However, it still remains a challenge to produce artificial photonic elastomers with desired optical and mechanical properties. Here, the generation of metallosupramolecular polymer-based photonic elastomers with tunable mechanical strength, angle-independent structural color, and self-healing capability is reported.

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In this report, we demonstrate the metal ion coordination-induced morphological transition of block copolymer assemblies under three-dimensional (3D) confinement. Polystyrene- block-poly(4-vinyl pyridine) (PS- b-P4VP) aggregates with various morphologies can be obtained by emulsion-solvent evaporation in the presence of metal ions (e.g.

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In this work, we present a fast and efficient strategy for the preparation of responsive photonic hydrogels for aldehyde sensing by combining the self-assembly of monodisperse carbon-encapsulated FeO nanoparticles (NPs) and in situ photopolymerization of polyacrylamide (PAM) hydrogels. The responsive photonic hydrogels exhibit structural color variation after being treated with formaldehyde aqueous solution, which can be attributed to the chemical reaction between the amide groups in the hydrogels and the formaldehyde. We have also shown that the photonic hydrogels can be used to determine the concentration of formaldehyde and to differentiate aldehydes through a facile reflection spectra shift and color change.

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A simple yet efficient method is developed to manipulate the self-assembly of pH-sensitive block copolymers (BCPs) confined in emulsion droplets. Addition of acid induces significant variation in morphological transition (e.g.

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The melt viscosity of three-arm star polystyrene (S3PS)-Fe(3)O(4) nanoparticle composites was studied by means of rheological measurements. The arm molecular weight (M(a)) of S3PS (or radius gyration) and the particle size of Fe(3)O(4) (radius (R(p)): 3 nm and 44 nm) showed a strong influence on the melt viscosity behavior (at low shear frequencies) of S3PS-Fe(3)O(4) composites. The reinforcement (viscosity increase) was observed in the composites where the M(a) was higher than the M(c) of PS (M(c): the critical molecular weight for chain entanglement).

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Rheological behavior of three-arm and six-arm star polystyrene (SPS) with a small amount of polyhedral oligosilsesquioxane (POSS) was studied. Both linear oscillatory frequency sweep and steady state shear results of SPS/POSS composites showed the reduction of melt viscosity in the unentangled SPS matrix and the increase of viscosity in the entangled SPS matrix. In particular, when molecular weight of the arm (Ma) of SPS was smaller than the critical molecular weight for entanglement (Mc) of PS, the melt viscosity of SPS/POSS composites with low content of POSS was lower than that of pure SPS.

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Controlled chain-scission of polybutadiene (PB), polyisoprene, and poly(styrene-co-butadiene), induced by bis(cyclopentadienyl) zirconium hydrochloride (Cp(2)ZrHCl), was revealed at room temperature. The chain-scission reaction of linear PB was studied by means of GPC, NMR spectroscopy, and MALDI-TOF-MS. It was confirmed that the molecular weights of degraded products were quasi-quantitatively controlled by Cp(2)ZrHCl loading, irrespective of the starting PB, whereas the microstructure of PB chains was crucial to the scission reaction.

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Using electrophoretic mobility shift assays, we examined sequence-specific binding of DEK, a potential autoantigen in juvenile rheumatoid arthritis, to conserved Y-box regulatory sequences in class II MHC gene promoters. Nuclear extracts from several cell lines of different phenotypes contained sequence-specific binding activity recognizing DRA, DQA1*0101, and DQA1*0501 Y-box sequences. Participation of both DEK and NF-Y in the DQA1 Y-box binding complex was confirmed by 'supershifting' with anti-DEK and anti-NF-Y antibodies.

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